A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866879



Internal ID22641814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43738565..43742369hg38UCSC Ensembl
chr12:44132368..44136172hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg383805
hg193805
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459855
Samples
Known GenesPUS7L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866879
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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